Quality System Specialist

About the role

We are seeking a Quality System Specialist to support the implementation and maintenance of our Quality Management System (QMS) within a leading healthcare organization focused on plasma‑derived medicines. The role ensures regulatory compliance, drives continuous improvement, and collaborates across functions to uphold the highest quality standards.

Key responsibilities

• Monitor and maintain the Quality Management System (QMS).
• Follow up on deviation investigations and CAPA activities.
• Ensure compliance with GMP and other regulatory requirements.
• Track quality KPIs and prepare performance reports.
• Support internal and external audits.
• Review and update quality documentation and SOPs.
• Coordinate with cross‑functional teams to resolve quality issues.
• Assist in implementing continuous improvement initiatives.

Required profile

• Bachelor's degree in Pharmacy, Science, Biotechnology or a related health field.
• Minimum 2 years of experience in Quality Systems within the pharmaceutical industry.
• Experience working under GMP regulations (preferred).
• Strong communication, analytical and problem‑solving abilities.
• High attention to detail and ability to manage multiple priorities.
• Fluent in English and Arabic.
• Ability to work effectively in a highly regulated environment and collaborate with cross‑functional teams.

Required skills

• Knowledge of Quality Management Systems (QMS).
• Experience with CAPA, deviation management and SOP maintenance.
• Understanding of GMP and pharmaceutical quality standards.
• Proficiency in Microsoft Office applications.